Can a Mind-Body group program break the cycle of domestic violence?
NCT ID NCT07747766
First seen Aug 05, 2026 · Last updated Aug 06, 2026 · Updated 1 time
Summary
This study tests whether a group-based program can help people who have been court-mandated after using violence with an intimate partner. The program combines themed lessons, experiential exercises like meditation and psychodrama, and group discussion to address stress, trauma, and substance use. Half of the participants will receive the program, while the other half will not, allowing researchers to compare outcomes. The goal is to see if this approach is feasible and acceptable, and whether it can reduce violence and improve well-being.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A group-based behavioral program combining themed curriculum, experiential exercises, and group discussion to address trauma and stress linked to intimate partner violence.
- What this could lead to
- If successful, this program could offer a new way to help people who have used violence in relationships break the cycle, reducing harm and improving family well-being.
- What could go wrong
- This is a small early-stage study focused on feasibility, not proof of effectiveness. Results may not generalize, and the program's impact on violence reduction remains uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 48 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Male participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Must be male-identifying or prefer to be in a male-identifying group; * Must be a resident of Washington state; * Must be court-referred to a treatment program for using violence with an intimate partner; * Have sufficient English fluency and literacy skills to understand the consent process, procedures and questionnaires and have the ability to provide written informed consent; * Have access to the internet and an electronic device with adequate data capacity; to complete questionnaires online and attend online video conference groups; * Must be available and willing to attend at least 17 out of 20 scheduled online group sessions; and * Must be available and willing to complete the online computerized assessments, and phone interviews. Exclusion Criteria: * Insufficiently stable housing or internet connection to be able to join at least 17 group sessions; * Current participation in another experimental research study; * Expected medical hospitalization in the next six months from study enrollment period; * Current or expected physical incarceration (excluding house arrest or other forms of electronic monitoring) in the next six months from study enrollment period; * Inpatient hospitalization for mental health, substance use, suicide attempt or self-harm within past three months; * Inability to participate safely in the study intervention and without disrupting the group (in the opinion of principal investigator OR meeting any of the following criteria) * Past year history of a psychotic disorder or clinician confirmed active psychosis assessed by the Structured Clinical Interview for DSM-5 (SCID-5); * Bipolar I disorder history or current severe level of mania assessed by the Structured Clinical Interview for DSM-5 (SCID-5); * Acute suicidality with intent will be excluded from the study (Structured Clinical Interview for DSM-5 \[SCID-5\]); * High levels of Psychopathy as defined by self-report psychopathy checklist (SRP-4); * Self-injurious behavior in past three months will require clinical assessment prior to participation in the program; * Acute homicidality with plan and/or intent; * Inability to join a group without intoxication. * Prior experience or exposure with Internal Family Systems (e.g. IFS therapy, IFS groups or retreats, current IFS practice, etc.)
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Cambridge Health Alliance Center for Mindfulness and Compassion
Malden, Massachusetts, 02148, United States
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Waterland Counseling
Tumwater, Washington, 98512, United States
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